In today’s tightly regulated healthcare environment, ensuring compliance with UK standards is more crucial than ever for medical device manufacturers worldwide. That’s where UK Responsible Person steps in—providing comprehensive support for UK Medical Device Registration and ensuring a smooth, legally compliant market entry for non-UK manufacturers.

April 10, 2025

London, United Kingdom

Specialising in post-Brexit regulatory requirements, UK Responsible Person offers a complete compliance solution tailored to meet the stringent expectations of the UK Medicines and Healthcare products Regulatory Agency (MHRA). With expert guidance and hands-on support, we make it possible for global medical brands to maintain continuity, avoid market disruption, and fully meet their obligations under UK law.

Our primary focus includes acting as the legally designated UK Responsible Person, handling all regulatory interactions, documentation reviews, and updates required for both general and in-vitro diagnostic devices. We also support manufacturers in navigating the complex process of UK Medical Device Registration, ensuring that every submission is accurate, timely, and fully compliant.

Seamless UKCA Registration and Ongoing Regulatory Support

As the UK continues to develop its independent regulatory framework, our role becomes even more vital. Our dedicated team ensures your product remains market-ready with expert support across the full lifecycle—from initial compliance checks to post-market surveillance and label review.

One of our key strengths lies in facilitating UKCA registration services, helping manufacturers transition smoothly from CE marking to UKCA marking. With the UK’s unique requirements now in full force, having a reliable partner with in-depth knowledge of the UKCA framework is no longer optional—it’s essential.

Our experienced consultants manage all aspects of UKCA registration services, from confirming classification to verifying technical documentation, ensuring your products meet the latest MHRA standards.

Why Work With Us?

1. Regulatory Expertise: We bring years of hands-on experience and stay updated with every policy change so you don’t have to.

2. Responsive Service: We pride ourselves on quick, clear communication and fast turnaround times.
Cost-Effective Solutions: Our pricing is transparent and competitive, designed with your operational budget in mind.

3. Trusted by Global Brands: Clients from across the EU, US, and Asia trust us to be their eyes and ears in the UK regulatory space.

About UK Responsible Person

UK Responsible Person is an established compliance service provider based in London, supporting international medical device manufacturers with tailored solutions for UK Medical Device Registration and regulatory representation. Our services are designed to remove the guesswork and help clients navigate post-Brexit UK market entry with confidence.

Whether you're launching a new product or maintaining an existing portfolio, let us help you stay compliant, competitive, and confident in the UK healthcare market.

Contact Details:

UK Responsible Person Ltd.

Email: [email protected]

Website: https://ukresponsibleperson.net